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{"type":"standard","title":"Hydroxylated lecithin","displaytitle":"Hydroxylated lecithin","namespace":{"id":0,"text":""},"wikibase_item":"Q15411032","titles":{"canonical":"Hydroxylated_lecithin","normalized":"Hydroxylated lecithin","display":"Hydroxylated lecithin"},"pageid":31160956,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/1/16/Hydroxylated_Lecithin.png/330px-Hydroxylated_Lecithin.png","width":320,"height":474},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/commons/1/16/Hydroxylated_Lecithin.png","width":394,"height":583},"lang":"en","dir":"ltr","revision":"1042330746","tid":"7b72d897-0d78-11ec-991a-239ef184846e","timestamp":"2021-09-04T12:06:06Z","description":"Chemical compound","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/Hydroxylated_lecithin","revisions":"https://en.wikipedia.org/wiki/Hydroxylated_lecithin?action=history","edit":"https://en.wikipedia.org/wiki/Hydroxylated_lecithin?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:Hydroxylated_lecithin"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/Hydroxylated_lecithin","revisions":"https://en.m.wikipedia.org/wiki/Special:History/Hydroxylated_lecithin","edit":"https://en.m.wikipedia.org/wiki/Hydroxylated_lecithin?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:Hydroxylated_lecithin"}},"extract":"Hydroxylated lecithin is chemically modified lecithin. It is made by treating lecithin with hydrogen peroxide and an organic acid such as acetic or lactic acid. In the process, some of the organic acid becomes peroxy acid. The peroxy acid reacts with olefins in the fatty acid side chains creating intermediate epoxides. The epoxides react further with water, organic acid, or peroxy acid, to ultimately form vicinal diols. Because the natural fatty acid olefins have (Z)-configurations, the resulting vicinal diols have anti stereochemical configurations.","extract_html":"

Hydroxylated lecithin is chemically modified lecithin. It is made by treating lecithin with hydrogen peroxide and an organic acid such as acetic or lactic acid. In the process, some of the organic acid becomes peroxy acid. The peroxy acid reacts with olefins in the fatty acid side chains creating intermediate epoxides. The epoxides react further with water, organic acid, or peroxy acid, to ultimately form vicinal diols. Because the natural fatty acid olefins have (Z)-configurations, the resulting vicinal diols have anti stereochemical configurations.

"}

{"slip": { "id": 159, "advice": "What's stopping you?"}}

{"fact":"Heat occurs several times a year and can last anywhere from 3 to 15 days.","length":73}

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{"fact":"Smuggling a cat out of ancient Egypt was punishable by death. Phoenician traders eventually succeeded in smuggling felines, which they sold to rich people in Athens and other important cities.","length":192}

{"slip": { "id": 120, "advice": "A nod is as good as a wink to a blind horse."}}

{"fact":"Owning a cat is actually proven to be beneficial for your health.","length":65}

{"fact":"Purring does not always indicate that a cat is happy and healthy - some cats will purr loudly when they are terrified or in pain.","length":129}

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{"type":"standard","title":"Inverse agonist","displaytitle":"Inverse agonist","namespace":{"id":0,"text":""},"wikibase_item":"Q1671731","titles":{"canonical":"Inverse_agonist","normalized":"Inverse agonist","display":"Inverse agonist"},"pageid":1200465,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/6/6c/Inverse_agonist_3.svg/330px-Inverse_agonist_3.svg.png","width":320,"height":176},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/6/6c/Inverse_agonist_3.svg/534px-Inverse_agonist_3.svg.png","width":534,"height":293},"lang":"en","dir":"ltr","revision":"1210969737","tid":"66ffbaa5-d6c5-11ee-8d1c-c8b5cb4a0a8b","timestamp":"2024-02-29T05:43:02Z","description":"Agent in biochemistry","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/Inverse_agonist","revisions":"https://en.wikipedia.org/wiki/Inverse_agonist?action=history","edit":"https://en.wikipedia.org/wiki/Inverse_agonist?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:Inverse_agonist"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/Inverse_agonist","revisions":"https://en.m.wikipedia.org/wiki/Special:History/Inverse_agonist","edit":"https://en.m.wikipedia.org/wiki/Inverse_agonist?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:Inverse_agonist"}},"extract":"In pharmacology, an inverse agonist is a drug that binds to the same receptor as an agonist but induces a pharmacological response opposite to that of the agonist.","extract_html":"

In pharmacology, an inverse agonist is a drug that binds to the same receptor as an agonist but induces a pharmacological response opposite to that of the agonist.

"}